CA2000146A1 - Polyglycidyl esters, their preparation and their use in thermosetting compositions - Google Patents

Abstract

A B S T R A C T

NOVEL POLYGLYCIDYL ESTERS, THEIR PREPARATION AND THEIR USE IN
THERMOSETTING COMPOSITIONS

Polyglycidyl esters of general formula wherein R is H or CH3; A represents an alkylene group -CR2-CH2-wherein each R1 represents a C1-C4 alkyl group which may be the same or different, which group A is attached to the adjacent group B via the -CH2- group; n has a value in the range of from 0-10; m is 1 or 2; for m is 1 B represents a group -SOp- or a group -SOp-Q-SOp- wherein p is 0, 1 or 2, and Q is a linear or branched alkylene group having from 2-10 carbon atoms, for m is 2 B represents a group (SOp-CH2)2-CH-SOp-, wherein p has the same meaning as hereinbefore.
The polyglycidyl esters may be used as reactive diluent and/or as binder component in thermosetting systems.

Description

2~ 6 T ~40 NOVEL POLYGLYCIDYL ESTERS, THEIR PREPARATION AND THEIR USE IN
THERMOSETTING COMPOSITIONS

This invention relates to novel polyglycidyl esters, a process for their preparation and their use in thermosetting compositions, particularly for use in solventless coatings and composites.
Diglycidyl esters of linear dicarboxylic acids such as adipic and sebacic acid are known e.g. from US Patent 3,053,855. Although such polyglycidyl esters and the products based thereon have been found to have very good outdoordurability performance properties, they suffer from a major deficiency, i.e. insufficient hydrolytic stability. Diglycidyl esters having improved hydrolytic stability have been described in German Published Patent Application 1942836, and are based on branched dicarboxylic acids having a linear Cl-C10 alkylene chain carrying 2-3 Cl-C4 alkyl substituents, special attention being focussed on the diglycidyl esters of 2,2,4- and 2,4,4- trimethyladipic acid. The improved hydrolytic stability of these diglycidyl esters being no doubt related to the presence of an ~-carbon atom, with respect to the carbonyl group, carrying one or two lower alkyl substituents. In this conte~t it may be expected that polyglycidyl esters based on polycarboxylic acids whereln each of the ~-carbon atoms is di-substituted with a lower alkyl group, e.g. a methyl group, should be of great interest.
As a result of continuing and extensive research and experimentation, there was surprisingly found that it is possible to prepars such polyglycidyl esters, based on polycarboxylic acids carrying two alkyl substituents on each of the ~-carbon atoms.
These polyglycidyl esters are novel compounds.
The invention pro~ides therefore polyglycidyl esters of general formula O O O O O O
(CH2!CR-CH2-O-C-A~mB-A-C-O~C~l2-CRtOH)-CH2-O-C-A-B-A-C-O~nCH2-CR-CH2 I

~n~ 6 wherein R is }I or CH3; A represents an alkylene group -CRl-CH2^
wherein each R represents a Cl-C4 alkyl group which may be the same or different, which group A is attached to the adjacent group B via the -~H2- group; n has a value in the range of from 0-lO; m is l or 2; for m is l B represents a group -S0 - or a group -S0 -Q-S0 - wherein p is 0, l or 2, and Q is a linear or branched alkylene group having from 2-lO carbon atoms, for m is 2 B
represents a group ~S0 -CH~)2-CH-S0 -, wherein p has the same meaning as hereinbefore.
In the context of the present invention the term polyglycidyl ester refers to glycidyl esters having on average more than one glycidyl ester group per molecule.
Dependin~ on the type of acid from which they have been derived, as well as on their molecular weight, the polyglycidyl esters of the present invention may vary from low-viscosity, oil-type liquids to highly viscous or semi-solid products. The low-viscosity polyglycidyl esters may suitably be used as reactive diluent in thermosetting and chemically crosslinkable systems. The higher viscosity products may be used e.g. as a binder component in coating compositions and/or composites. A further potential outlet envisaged for these glycidyl esters is as stabilizer e.g. in polymers. Except for a difference in viscosity and physical state, the polyglycidyl esters of general formula I will include products which may vary strongly in oeher characteristics such as glass-transition temperature (Tg) and hydrolytic stability. Forapplications which have a certain minimum requirement regarding the Tg a preferred class of such polyglycidyl esters are those wherein B is -S0 -Q-S0 - and Q is an ethylene group, or wherein B is -SO -.
Especially preferred are such polyglycidyl esters wherein p is l or 2 and more preferably p is 2. A class of polyglycidyl esters of general formula I of which ~he molecular structure may provide a positive contribution towards the Tg of said polyglycidyl esters or the products derived therefrom, are those wherein each Rl is -CH3.
For applications wherein the requirements regarding hydrolytic ~oo~

stability are very strict, preferred polyglycidyl esters are those wherein p is 0.
Although in theory the number of glycidyl groups per molecule of polyglycidyl ester will be equivalent to the functionality o~
the polycarboxylic acid on which they are based, in practice and depending the method of preparation, this number may be somewhat lower, the difference being made up by e.g. ~-glycol groups, i.e.
hydrolysed glycidyl groups, chlorohydrin groups and carboxyl groups.
The preparation of the polyglycidyl esters of the present invention may conveniently be conducted by known processes for the preparation of polyglycidyl esters e.g. such as those which have been described in the hereinbefore mentioned German Patent Application, i.e.:
a) the reaction of the alkali metal salt of a suitable polycar-boxylic acid with an excess of an epihalohydrin or a ~-methyl-epihalohydrin and subsequently separating off the co-formed alkali metal halogenide, bl) the reaction of a polycarboxylic ac:Ld with an excess of an epihalohydrin or a ~-methylepihalohydrill, generally >2 mol of epihalohydrin per carboxyl group, in the presence of a suitable catalyst such as a tertiary amine, a quaternary ammonium salt or an ion-exchange resin, whereby the intermediately formed halohydrin group is converted to an epoxy group under the production of the corresponding glycerindihalogenhydrin as a result of the reaction between the halohydrin formed and the excess of epihalohydrin or ~-methylepihalohydrin, and b2) a reaction between a polycarboxylic acid and epihalohydrin or ~-methylepihalohydrin in the presence of a tertiary amine or a quaternary ammonium salt and employing a dehydrohalogenation-agent such as water-free sodium hydroxide or related inorganic compounds Preferably the epihalohydrin and/or the ~-methylepihalohydrin which may be used in the preparation of the polyglycidyl esters of the present invention are epichlorohydrins, epichlorohydrin being especially preferred.

, ~ .

20~

It will be understood by those skilled in the art that the value for n will be largely determined by the nature of the process used for the preparation of the polyglycidyl esters as well as by the excess of epihalohydrin compound employed. Generally the polyglycidyl esters will be a mixture oE such esters having different values for n. If desirable it is also possible to prepare such polyglycidyl esters by reaction of a polycarboxylic acid of general formula II, as given hereinafter, with a molar excess of a polyglycidyl ester as hereinbefore described e.g. a polyglycidyl ester of general formula I for which n-o, in the presence of a suitable catalyst.
The polycarboxyiic acids which may be employed in the preparation of the polyglycidyl esters of the present invention are polycarboxylic acids of general formula O O
(H0-C-A3mB-A-C-OH II
wherein A, B and m have the same meaning as hereinbefore. Examples of polycarboxylic acids of general formula II incl~tde thiodipivalic acid, sulfinyldipivalic acid, sulfonyldipivalic acid, ethane-1,2-bis(thiopivalic acid), ethane-1,2-bis(sulfinylpivalic acid), ethane-1,2-bis (sulfonylpivalic acid~, propane-1,2,3-tris(thiopivalic acid), propane-1,2,3-tris(sulfinylpivalic acid) and propane-1,2,3-tris(sulonylpivalic acid), butane-~
bis(thiopivalic acid), butane-1,~-bis(sulfinylpivalic acid) and butane-1,4-bis(sulfonylpivalic acid). Thiodipivalic acid is a preferred polycarboxylic acid of general formula II.
, 25 Polycarboxylic acids of general formula II, wherein B is -SO -(CH2)4-SO - or ~SO -CH2~2CH-SO -, are novel compounds.
The polycarboxylic acids of general formula II wherein B is -SO -Q-SOp- or ~SO -CH2~CH-SO - and p is O can conveniently be prepared e.g. by the reaction of chloropivalic acid with the appropriate alkanepolythiol having from 2-10 carbon atoms as described by A.C. Bellaart et al, Z. anorg.allg. Chem. 412, 155-160 (1975)-A preferred and novel method for the preparation of said polycarboxylic acids is via the reaction of the dialkali metal or diammonium salt of mercaptopivalic acid with the appropriate dihalogen alkane having from 2-10 carbon atoms, followed by acidification of the reaction product.
The preparation of thiodipivalic acid tp is 0 and B is -SOp-) can conveniently be conducted by stirring an aqueous emulsion of sodium chloropivalate for 24 hours at 20-23 ~C with an aqueous solution of sodium sulfide and subsequently acidifying the reaction medium to provide the thiodipivalate as a precipitate; this method is known. A preferred and novel method for the preparaeion of thiodipivalic acid is via the reaction of the dialkali metal or diammonium salt of mercaptopivalic acid with pivalolactone at a temperature in the range of from 0-25 C and preferably in the range of from 5-15 C followed by acidification of the reaction product.
The polycarboxylic acids of general formula II, wherein p is 1 or 2, may be prepared from the corresponding acids wherein p is 0 by reacting a dialkyl ester of such an acid e.g. diethyl thiodipivalate, as a solution in a blend of glacial acetic acid and acetic anhydride with the desired amount of hydrogen peroxide (30 ~m), which is added dropwise to said solution over a period of 3 hours. After removal of excess solvent the desired product may be isolated via acidification and recrystallization. This method is known. ~ith the polyglycidyl esters of general formula I wherein p is 1 or 2 there is more than one method for their preparation, e.g.:
~) glycidation of polycarboxylic acids of general formula II
wherein p has the value of 1 or 2, and b) glycidation of polycarboxylic acids of general formula II
wherein p is 0, followed by oxidation of the thio group(s)-containing polyglycidyl esters thus obtained, to the corresponding sulfinyl or sulfonyl group(s)-containing compounds by reacting a solution oi` e.g. diglycidyl thiodipivalate in dichloromethane and glacial acetic acid at -10 ~C with zn~ 6 stepwise-added benzyltriethyl ammonium permanganate for one hour.
After dilution with diethyl ether the reaction is stirred for 30 minutes, whereupon the mixture is filtered. After parifying the organic solution, the desired compound can be obtained via evaporation of the organic solvent.

Preparation of thiodipivalic acid To a stirred solution of 26 mol of the disodium salt of mercaptopivalic acid in l0.l l of water and having a temperature of 10 10 CI 2600 g (26 mol) of pivalolactone was added over 4 hours and at such a rate that the temperature of the reactor contents was maintained at approximately l0 C. As the reactor contents tended to solidify a further l,5 l water was added during the pivalolactone addition. Upon completion of the lactone addition the solution was stirred for a further 2 h. The reactor contents were acidified with concentrated hydrochloric acid (6050 ml) to arrive at a pH 3. The thick white precipitate Eormed, was separated ~y filtration. The solid mass was stirred in 8 1 water and refiltered.
The crude damp product at this stage weighed 7308 g. A small portion (34.39 g) was dried to give a white powder (27.75 g) which had a m.p. 155-157 C (lit. 163-164 C) i.e. a yield of crude thiodipivalic acid (TDPA) of 5465 g~ (9~%). The crude acid was recrystallized from an industlial methylated spirit (IMS)/water mixture (4.5/10 1) at reflux. The solution was allowed to cool for two days, and the recrystallized TDPA was separated by filtration and washed with water/IMS 100:45 v/v. After drying at 90 C / 0,5 mm, 4401 g of pure TDPA was obtained ~72.3 % yield on lactone) having a m.p. 163-164 C.
Analysis found: C, 50.7; H, 7.8; S, 13.8~o Calculated for CloHl804S C, 51 - 2; H~ 7 - 8; S ~ 13 - 8% -Acid value: 474 mg KOH/g.
Example II
Preparation of butane-l, 4 ~ bis(thiopivalic acid).
An aqueous solution of the disodium salt of mercaptopivalic acid (MPA) was prepared under nitrogen from MPA (2 mol, 2S8.4 g), sodium hydroxide (4 mol, 160 g) and water (800 ml). The solution was stirred at 70 C and 1,4-dichlorobutane (1 mol, 91.5 g) was added over 20 min, during which time the temperature of the turbid reaction mixture remained at 70-80 C. The reaction mixture was stirred until all the dichlorobutane had reacted (approx. 9O min), as a result of which the turbidity disappeared and the temperature had increased to lOO C. The solution was stirred for a further 15 minutes at lOO C, cooled, and acidified dropwise with concentrated hydrochloric acid (l~O ml). The precipitated solid was filtered off, sucked-dry and recrystallized from diethyl ether / 30-40 C
boiling range petroleum spirit to give ehe pure acid, as a white solid, in 86.5% yield, M.p. 95.5-96 C, equivalent weight 162.1.
Analysis found: C, 51.8; H, 8.1; S, 20.2~.
14 26 4 2 ' ; ' ; ' ~-E~ample III
Preparation of propane-1,2,3-tris(thiopivalic ac:id).
Propane-1,2,3-tris(thiopivalic acid) was prepared following the method as described in e~ample II and employing 1 mol of 1,2,3-trichloropropane, 3 mol MPA and 6 mol NaOH. After recrystallization the acid was obtained in a 83 % yield.
M.p: 118-121 C, equivalent weight 148.3.
Analysis found: C, 48.8; H, 7.3; S, 22.9~.
Calculated for C18~1326S3 C~ 49 1; ~1~ 7-3; S~ 21-8~-Example IV
Preparation of sulfonyldipivalic acid (SDPA) Tungsten oxide (10 g, 0.04 mol) was stirred as a suspension in water (5 1) at 50 C. A concentrated aqueous solution of sodium hydroxide was added dropwise to give an alkaline solution when all the oxide had dissolved. The solution was acidified to a pH 5-6 with glacial acetic acid to liberate tungstic acid, which compound is used as a catalyst in the preparation of the SDPA.
Thiodipivalic acid (936.8 g, 4.0 mol) was added to the tungstic acid coneaining solution and the resulting slurry was stirred at 60 ~C. Next hydrogen peroxide (1000 ml of 30~ m) was added dropwise to the slurry. During the addition of the first 500 zo~

ml (over 100 min) the temperature remained at 72-73 C without external heating. During the addition of the remainder of the hydrogen peroxide (over 40 min) external heating was required to keep the temperature in the range of from 75-85 C. Subsequently the slurry was stirred at 8S-89 C for 24 hours and then cooled.
Crude SDPA was separated by filtration and washed free of peroxide with water. The crude SDPA was obtained in 90 % yield, m.p. 237-240 C. After recrystalli~ation from glacial acetic acid (5 1~, washing with petroleum spirit (40-60 C boiling range) and drying at 100 C/5 mm Hg, there was obtained 866 g (81,5 %) of pure SDPA; mp 239.5-240.5 C.
Analysis Found: C, 44.6; H, 6.8; S, 12.2~
Calculated for CloH1806S: C, 45.1; H, 6.8; S, 12.1%
Acid value 426 mg KOH/g.
~xample V
Preparation of diRlycidyl thiodipivalate The disodium salt of thiodipivalic acid was prepared by adding 35,1 g (0.15 mol) thiodipivalic acid to a solution of 11,79 g sodium hydroxide in 58.8 ml water, and stirring this mixture for about 15 minutes. This was followed by removing the water by means of evaporation at reduced pressure and further drying at 50-75 C and 100 mm Hg.
The disodium thiodipivalate was added to a stirred mixture of 215.0 g (2,32 mol) epichlorohydrin (ECH) and 0.91 g (2.82 x 10 mol) tetrabutyl ammonium bromide. Subsequently the mixture was refluxed with stirring, for 4 hours (on an oil bath 120 C) and cooled to 40 C and filtered. The excess ECH was removed by evaporation at a temperature of up to 120 C and a pressure of 15 mm Hg. The residue was added to 147 ml toluene, which was followed by the addition of 1.88 g sodium hydroxide in 27,5 ml water The resulting two layer system was heated for 15 min. on an oil bath at 100 C. The organic layer was separated off and washed with 300 ml of an aqueous 3 % m NaH2PO4 solution, which was followed by washing with water, drying over MgSO4 and filtering.
The solvent was evaporated under reduced pressure (15 mm Hg).

2~

Vacuum distillation of the residue resulted in 39.4 g (yield 76 %) of a pale-yellow oil having a b.p. 167 C/0.03 mm Hg and a viscosity of 91 mPa.s. H NMR and 13C-NMR indicated the product to be diglycidyl thiodipivalate. The epoxy content was found to be 96.1 ~ of the theoretical amount and which epoxy content did not change during storage at 40 C of 40 days.
Example VI
Preparation of diglycidyl sulfonyldipivalate 346 mg diglycidyl thiodipivalate (1 mmol) was dissolved in 10 ml ~ dichloromethane which was followed by the addition of 1 g glacial acetic acid. The stirred solution was cooled to -10 C with the aid of an ice/salt bath. Subsequently 684 mg benzyltriethyl ammonium permanganate was added stepwise i.e. 7 additions of approximately 98 mg, at a rate of 1 addition per min. After stirring the mixture ~5 for one hour the ice/salt bath was removed and 20 ml diethyl ether was added and after stirring a further 30 min. the mixture was filtered. The organic solution was shaken twice with 15 ml water and once with 15 ml of an aqueous 5 ~ m NaHC03 solution, dried with MgS04 and filtered. Finally the solvent was removed by evaporation in a film evaporator resulting in 240 mg of diglycidyl sulfonyl-dipivalate. The presence of the sulphorlyl groups being confirmed by Infra Red Spectroscopy.
Example VII
Preparation of crosslin~ed diglyci.dyl esters of thiodipivalic acid The diglycidyl ester of thiodipivalic acid as prepared in Example V
was mixed with isophorone diamine (IPD) and diphenyldiamino methane (DDM) in amounts and under conditions as indicated in Table 1 hereinafter. The mixtures were trans~erred to an aluminium cup (~ 5 cm) which had been pretreated with a silicon-based release agent (ex Dow Corning). The contents of the cups were heated for 1 h at 100 C, followed by 1 h at 125 C and finally for 4 h at 175 C.
The diglycidyl ester /IPD mixture was also applied as a 25 ~m film on a phosphatized steel strip with the aid of a film applicator and subsequently heated in a nitrogen atmosphere for 90 min at 175 C.

20~Q~ ~

After curing all castings were hard, clear light coloured systems oE which the Tg values have been included in Table 1. The IPD base film furthermore demonstrated very good adhesion properties to the metal substrate and a high gloss.
Table 1 ApplicationCasting Casting Film . . -Diglycidyl ester g 2.415 2.333 3.14 IPD g 0.585 - 0.76 DDM g - 0.667 Mixing temp. C 20 100 20 Tg after curing C 77 79 . .
The individual compounds were heated separately to 100 C
before mixing.

Claims (8)

1. Polyglycidyl esters of general formula wherein R is H or CH3; A represents an alkylene group -CR2-CH2-wherein each R1 represents a C1-C4 alkyl group which may be the same or different, which group A is attached to the adjacent group B via the -CH2- group; n has a value in the range of from 0-10; m is 1 or 2; for m is 1 B represents a group -SOp- or a group -SOp-Q-SOp- wherein p is 0, 1 or 2, and Q is a linear or branched alkylene group having from 2-10 carbon atoms, for m is 2 B represents a group ?SO-CH2)2-CH-SOp-, wherein p has the same meaning as hereinbefore.

2. Polyglycidyl esters as claimed in claim 1, wherein B is -SOp-Q-SOp- and Q is an ethylene group.

3. Polyglycidyl esters as claimed in claim 1, wherein B is -SOp-.

4. Polyglycidyl esters as claimed in any one of claims 1-3, wherein each R1 is CH3.

5. A process for the preparation of polyglycidyl esters as claimed in any one of claims 1-4, wherein a polycarboxylic acid of general formula wherein A, B and m have the same meaning as hereinbefore is reacted with an excess of an epihalohydrin or a .beta.-methylepihalo-hydrin by known methods.

6. A process as claimed in claim 5, wherein the polycarboxylic acid is thiodipivalic acid and the epihalohydrin is epichlorohydrin.

7. Polycarboxylic acids of general formula

8. Butane-1,4-bis(thiopivalic acid), propane-1,2,3-tris(thio-pivalic acid), diglycidyl thiopivalate and diglycidyl sulfonyl-dipivalate.